ProfileGDS1065 / 218124_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 71% 82% 71% 92% 83% 77% 89% 77% 84% 77% 80% 66% 80% 72% 74% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1110.471
GSM24653Normal subject 2189.382
GSM24654Normal subject 3137.671
GSM24655A3243G-MELAS subject 1298.492
GSM24656A3243G-MELAS subject 2217.683
GSM24657A3243G-MELAS subject 3232.777
GSM24658A3243G-MELAS subject 4327.889
GSM24659A3243G-PEO subject 1109.577
GSM24660A3243G-PEO subject 221284
GSM24661A3243G-PEO subject 3104.977
GSM24662A3243G-PEO subject 4151.880
GSM24663mtDNA "Common"-deletion subject 191.766
GSM24664mtDNA "Common"-deletion subject 2313.180
GSM24665mtDNA "Common"-deletion subject 3171.772
GSM24666mtDNA "Common"-deletion subject 4212.174